Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1
Introduction: To evaluate myocardial strain and extracellular volume in myotonic dystrophy type 1 (DM1) patients as potential imaging biomarkers of subclinical cardiac pathology.Materials and methods: We retrospectively analyzed 9 DM1 patients without apparent cardiac disease who had undergone cardi...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2020-03-01
|
Series: | Frontiers in Neurology |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fneur.2020.00192/full |
id |
doaj-3e34543a147c4b9bbc317eb1d83dba35 |
---|---|
record_format |
Article |
spelling |
doaj-3e34543a147c4b9bbc317eb1d83dba352020-11-25T03:08:08ZengFrontiers Media S.A.Frontiers in Neurology1664-22952020-03-011110.3389/fneur.2020.00192525516Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1Marco Alì0Marco Alì1Caterina Beatrice Monti2Luca Melazzini3Rosanna Cardani4Barbara Fossati5Barbara Fossati6Michele Cavalli7Kelvin Chow8Francesco Secchi9Francesco Secchi10Giovanni Meola11Giovanni Meola12Giovanni Meola13Francesco Sardanelli14Francesco Sardanelli15Unit of Diagnostic Imaging and Stereotactic Radiosurgery, C.D.I. Centro Diagnostico Italiano S.p.A., Milan, ItalyUnit of Radiology, IRCCS Policlinico San Donato, San Donato Milanese, ItalyPhD Course in Integrative Biomedical Research, Department of Biomedical Sciences for Health, University of Milan, Milan, ItalyPhD Course in Integrative Biomedical Research, Department of Biomedical Sciences for Health, University of Milan, Milan, ItalyLaboratory of Muscle Histopathology and Molecular Biology, IRCCS Policlinico San Donato, San Donato Milanese, ItalyUnit of Neurology, IRCCS Policlinico San Donato, San Donato Milanese, ItalyDepartment of Neurorehabilitation Sciences, Casa di Cura del Policlinico, Milan, ItalyPostgraduate School in Neurology, University of Milan, Milan, ItalySiemens Medical Solutions USA Inc., Chicago, IL, United StatesUnit of Radiology, IRCCS Policlinico San Donato, San Donato Milanese, ItalyDepartment of Biomedical Sciences for Health, University of Milan, San Donato Milanese, ItalyUnit of Neurology, IRCCS Policlinico San Donato, San Donato Milanese, ItalyDepartment of Neurorehabilitation Sciences, Casa di Cura del Policlinico, Milan, ItalyDepartment of Biomedical Sciences for Health, University of Milan, San Donato Milanese, ItalyUnit of Radiology, IRCCS Policlinico San Donato, San Donato Milanese, ItalyDepartment of Biomedical Sciences for Health, University of Milan, San Donato Milanese, ItalyIntroduction: To evaluate myocardial strain and extracellular volume in myotonic dystrophy type 1 (DM1) patients as potential imaging biomarkers of subclinical cardiac pathology.Materials and methods: We retrospectively analyzed 9 DM1 patients without apparent cardiac disease who had undergone cardiac magnetic resonance at our center. Patients were age- and sex-matched with healthy controls. The Mann-Whitney U test was used to compare cardiac strain between the two groups. The t-test was used to compare the extracellular volume obtained in DM1 patients with that in healthy subject. Spearman's ρ was used for studying the associations among imaging parameters.Results: Global cardiac strain (median −19.1%; IQR −20.5%, −16.5%) in DM1 patients was lower (p = 0.011) than that in controls (median−21.7%; IQR−22.7%,-21.3%). Global extracellular volume in DM1 patients (median 32.3%; IQR 29.3%,36.8%) was significantly (p = 0.008) higher than that reported in literature in healthy subjects (median 25.6%; IQR 19.9%,31.9%). Global cardiac strain showed a strong, positive correlation with septal strain (ρ = 0.767, p = 0.016) and with both global (ρ = 0.733 p = 0.025) and septal extracellular volume (ρ = 0.767, p = 0.016).Discussion: The increase in cardiac extracellular volume and decrease in strain are signs of early cardiac pathology in DM1. Physicians dealing with DM1 may take into consideration cardiac magnetic resonance as a screening tool to identify early cardiac involvement in this condition.https://www.frontiersin.org/article/10.3389/fneur.2020.00192/fullmyotonic dystrophycardiac magnetic resonancemyocardial strain imagingextracellular volumecardiac fibrosis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Marco Alì Marco Alì Caterina Beatrice Monti Luca Melazzini Rosanna Cardani Barbara Fossati Barbara Fossati Michele Cavalli Kelvin Chow Francesco Secchi Francesco Secchi Giovanni Meola Giovanni Meola Giovanni Meola Francesco Sardanelli Francesco Sardanelli |
spellingShingle |
Marco Alì Marco Alì Caterina Beatrice Monti Luca Melazzini Rosanna Cardani Barbara Fossati Barbara Fossati Michele Cavalli Kelvin Chow Francesco Secchi Francesco Secchi Giovanni Meola Giovanni Meola Giovanni Meola Francesco Sardanelli Francesco Sardanelli Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 Frontiers in Neurology myotonic dystrophy cardiac magnetic resonance myocardial strain imaging extracellular volume cardiac fibrosis |
author_facet |
Marco Alì Marco Alì Caterina Beatrice Monti Luca Melazzini Rosanna Cardani Barbara Fossati Barbara Fossati Michele Cavalli Kelvin Chow Francesco Secchi Francesco Secchi Giovanni Meola Giovanni Meola Giovanni Meola Francesco Sardanelli Francesco Sardanelli |
author_sort |
Marco Alì |
title |
Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 |
title_short |
Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 |
title_full |
Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 |
title_fullStr |
Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 |
title_full_unstemmed |
Rare Disease: Cardiac Risk Assessment With MRI in Patients With Myotonic Dystrophy Type 1 |
title_sort |
rare disease: cardiac risk assessment with mri in patients with myotonic dystrophy type 1 |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Neurology |
issn |
1664-2295 |
publishDate |
2020-03-01 |
description |
Introduction: To evaluate myocardial strain and extracellular volume in myotonic dystrophy type 1 (DM1) patients as potential imaging biomarkers of subclinical cardiac pathology.Materials and methods: We retrospectively analyzed 9 DM1 patients without apparent cardiac disease who had undergone cardiac magnetic resonance at our center. Patients were age- and sex-matched with healthy controls. The Mann-Whitney U test was used to compare cardiac strain between the two groups. The t-test was used to compare the extracellular volume obtained in DM1 patients with that in healthy subject. Spearman's ρ was used for studying the associations among imaging parameters.Results: Global cardiac strain (median −19.1%; IQR −20.5%, −16.5%) in DM1 patients was lower (p = 0.011) than that in controls (median−21.7%; IQR−22.7%,-21.3%). Global extracellular volume in DM1 patients (median 32.3%; IQR 29.3%,36.8%) was significantly (p = 0.008) higher than that reported in literature in healthy subjects (median 25.6%; IQR 19.9%,31.9%). Global cardiac strain showed a strong, positive correlation with septal strain (ρ = 0.767, p = 0.016) and with both global (ρ = 0.733 p = 0.025) and septal extracellular volume (ρ = 0.767, p = 0.016).Discussion: The increase in cardiac extracellular volume and decrease in strain are signs of early cardiac pathology in DM1. Physicians dealing with DM1 may take into consideration cardiac magnetic resonance as a screening tool to identify early cardiac involvement in this condition. |
topic |
myotonic dystrophy cardiac magnetic resonance myocardial strain imaging extracellular volume cardiac fibrosis |
url |
https://www.frontiersin.org/article/10.3389/fneur.2020.00192/full |
work_keys_str_mv |
AT marcoali rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT marcoali rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT caterinabeatricemonti rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT lucamelazzini rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT rosannacardani rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT barbarafossati rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT barbarafossati rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT michelecavalli rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT kelvinchow rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT francescosecchi rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT francescosecchi rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT giovannimeola rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT giovannimeola rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT giovannimeola rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT francescosardanelli rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 AT francescosardanelli rarediseasecardiacriskassessmentwithmriinpatientswithmyotonicdystrophytype1 |
_version_ |
1724667344484040704 |